by Ursula Tschorn | Nov 20, 2017
eAF is short for Electronic Application Form. Since 1 January 2016 the eAF is mandatory to use for all new Marketing Authorisation Applications, Renewals and Variations within all procedures in Europe.
by Ursula Tschorn | Sep 13, 2017 | FDA, News
How will FDA introduce IDMP? FDA proposes structured data for the CMC Module 3 of the eCTD standard (Blog content by our partner Dieter Schlaps) A few days ago, FDA has circulated a remarkable document for commenting, entitled “Pharmaceutical Quality/Chemistry...
by Ursula Tschorn | Mar 21, 2017
Informationsstelle für Arzneimittelanbieter GmbH (IFA) Die IFA GmbH ist Informationsdienstleister für den deutschen Pharmamarkt und liefert Informationsdienste mit wirtschaftlichen, rechtlichen und logistischen Daten zu bundesweit in deutschen Apotheken erhältlichen...
by Ursula Tschorn | Mar 20, 2017
PHARMAZIE.COM is an international drug information provider for Health Care Professionals. It has been online since 1996, making it one of the oldest electronic drug catalogs in the Internet. It is reserved for medical specialists according to § 10 HWG...
by Ursula Tschorn | Mar 20, 2017
The National Competent Authorities (NCAs) are the national agencies for the evaluation of medicinal products
